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Distraction Screw 909-12

by Medline Industries, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00818614021409 UDI-DI Date26 Jan 2023ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Distraction Screw
Generic Name
Orthopaedic bone pin, non-bioabsorbable
Model / Reference
909-12
Primary DI / UDI-DI
00818614021409
FDA Product Code
LYQ
GMDN Term
Orthopaedic bone pin, non-bioabsorbable
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
Not in Commercial Distribution
Size
Length — 12 Millimeter

Other devices from Medline Industries, Inc.

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (6)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No